The GPT2 Gene Mental Retardation Autosomal Recessive Type 49 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the GPT2 gene, which have been linked to autosomal recessive intellectual disability type 49. This condition is characterized by developmental delays, learning disabilities, and possibly other neurological or physical abnormalities. The test is crucial for families seeking answers to genetic questions related to intellectual disabilities, allowing for better understanding, management, and planning for affected individuals' needs. The test is priced at 4400 AED, reflecting the sophisticated technology and expertise required to accurately analyze and interpret the genetic data. DNA Labs UAE, with its state-of-the-art facilities and experienced professionals, ensures a reliable and comprehensive assessment for those undergoing the test.
The NSUN2 gene is associated with a condition known as Mental Retardation, Autosomal Recessive Type 5 (MRD5). This condition is characterized by intellectual disabilities that can range from mild to severe, often accompanied by other neurological and physical abnormalities. The NSUN2 gene plays a crucial role in the proper development and function of the brain, and mutations in this gene can lead to the symptoms observed in MRD5.
To diagnose this condition accurately, genetic testing of the NSUN2 gene can be conducted. DNA Labs UAE offers a comprehensive genetic test specifically designed to identify mutations in the NSUN2 gene that are linked to Mental Retardation, Autosomal Recessive Type 5. The test is a critical tool for families seeking answers to developmental delays and intellectual challenges faced by their loved ones. It provides essential information for understanding the condition, potential interventions, and management strategies to improve the quality of life for those affected.
The cost of the NSUN2 gene test at DNA Labs UAE is 4400 AED. This investment covers the meticulous process of analyzing the genetic material to detect any abnormalities in the NSUN2 gene that could indicate the presence of MRD5. The test is conducted under the guidance of genetic specialists who ensure the accuracy and reliability of the results. Upon completion, a comprehensive report is provided, detailing the findings and their implications for the individual and their family. This report serves as a valuable resource for healthcare providers in devising a personalized care plan tailored to the specific needs of the patient.
The RAB40AL gene, also known as the Mental Retardation X-Linked (MRX) gene, plays a crucial role in cognitive development. Mutations in this gene are associated with X-linked mental retardation, a condition that affects intellectual functioning and may be accompanied by physical or psychiatric comorbidities. The RAB40AL Gene Mental Retardation X-Linked Genetic Test is a specialized diagnostic tool designed to detect mutations in the RAB40AL gene. This test is particularly relevant for families with a history of X-linked mental retardation, offering them a chance to understand their genetic makeup and the risk of passing the condition to their offspring.
The test is available at DNA Labs UAE, a leading facility in genetic testing and analysis. The cost of the RAB40AL Gene Mental Retardation X-Linked Genetic Test is 4400 AED. The process involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory to identify any genetic mutations associated with the condition. The results of this test can provide valuable information for genetic counseling, helping families make informed decisions about future pregnancies and the management of the condition in affected family members.
The SLC9A6 gene mental retardation X-linked syndromic Christianson type genetic test is a specialized diagnostic assessment designed to identify mutations in the SLC9A6 gene, which are linked to Christianson syndrome. This condition, also known as X-linked Angelman syndrome, is a rare genetic disorder that affects neurological development, leading to intellectual disability, epilepsy, and difficulties with speech and movement. The test is crucial for early diagnosis and management of the syndrome, enabling tailored therapeutic strategies and support for affected individuals and their families.
Performed at DNA Labs UAE, a leading facility in genetic testing, the test involves analyzing the patient's DNA to detect specific mutations in the SLC9A6 gene that are associated with Christianson syndrome. The process is thorough, leveraging advanced genetic sequencing technologies to ensure accurate and reliable results.
The cost of the SLC9A6 gene mental retardation X-linked syndromic Christianson type genetic test is 4400 AED. While the price may seem significant, the value of obtaining a precise diagnosis cannot be understated, as it opens the door to specialized care and interventions that can significantly improve the quality of life for those affected by the condition.
The UBE2A gene mental retardation X-linked syndromic Nascimento-type genetic test is a specialized diagnostic tool designed to identify mutations in the UBE2A gene, which are linked to Nascimento syndrome. This condition is a rare form of X-linked intellectual disability that affects males and is characterized by features such as developmental delay, intellectual disability, sparse hair, distinctive facial features, and other physical abnormalities. The test is crucial for accurate diagnosis, allowing for tailored care and management plans for affected individuals.
Performed at DNA Labs UAE, a leading facility in genetic testing, the test involves analyzing the patient's DNA to detect mutations in the UBE2A gene. Given the complexity of the test and the advanced technology employed, the cost is set at 4400 AED. This investment covers the comprehensive analysis required to ensure accurate results, providing essential information for families and healthcare providers in managing the condition and making informed decisions about care and support.
The ZDHHC9 Gene Mental Retardation X-Linked Syndromic Raymond Type Genetic Test is a specialized diagnostic procedure designed to identify mutations in the ZDHHC9 gene, which are linked to a rare form of X-linked mental retardation known as Raymond syndrome. This condition primarily affects males and is characterized by intellectual disability, speech and language delays, and sometimes physical abnormalities. The test involves analyzing the patient's DNA to detect any genetic anomalies that might be responsible for the syndrome.
Conducted at DNA Labs UAE, a leading facility in genetic testing and diagnostics, this test is essential for families seeking to understand the genetic basis of intellectual disabilities and related syndromes in their loved ones. It can also provide valuable information for genetic counseling and inform decisions regarding management and support for affected individuals.
The cost of the ZDHHC9 Gene Mental Retardation X-Linked Syndromic Raymond Type Genetic Test is 4400 AED. This investment covers the comprehensive analysis required to accurately identify the presence of genetic mutations associated with the condition. Given the complexity and specificity of the test, it represents a crucial step towards personalized care and intervention for those impacted by Raymond syndrome.
The IQSEC2 gene mental retardation X-linked type 1 genetic test is a specialized diagnostic procedure designed to identify mutations in the IQSEC2 gene, which is located on the X chromosome. This gene plays a crucial role in cognitive development and functioning. Mutations in the IQSEC2 gene are associated with a form of intellectual disability known as X-linked mental retardation type 1. This condition primarily affects males and is characterized by varying degrees of cognitive impairment, learning disabilities, and sometimes behavioral problems.
The test is conducted through a blood sample, where DNA is extracted and analyzed for any genetic anomalies present in the IQSEC2 gene. It is particularly recommended for families with a history of X-linked intellectual disability or for individuals showing symptoms related to cognitive developmental delays without a known cause.
Conducted at DNA Labs UAE, a facility known for its advanced genetic testing services, the IQSEC2 gene test is available for a cost of 4400 AED. This test not only aids in the diagnosis of X-linked intellectual disability but also helps in understanding the condition better, guiding treatment plans, and providing information important for family planning.
The MID2 Gene Mental Retardation X-Linked Type 101 Genetic Test is a specialized diagnostic procedure aimed at detecting mutations in the MID2 gene, which are linked to a form of intellectual disability known as X-Linked Mental Retardation Type 101. This condition primarily affects males and is characterized by various degrees of cognitive impairment, developmental delays, and sometimes physical anomalies. The MID2 gene plays a crucial role in the development and function of the nervous system, and mutations in this gene can lead to the aforementioned intellectual disabilities.
The test is conducted through a detailed analysis of the patient's DNA, which is extracted from a blood sample. State-of-the-art genetic sequencing technologies are employed to identify any alterations in the MID2 gene that are associated with the condition. This test is crucial for families seeking to understand the genetic basis of intellectual disabilities in their members, as it can provide definitive answers and guide towards appropriate management and therapy options.
The MID2 Gene Mental Retardation X-Linked Type 101 Genetic Test is available at DNA Labs UAE, a leading facility in genetic testing and analysis. The cost of the test is 4400 AED, reflecting the comprehensive nature of the analysis and the specialized expertise required to interpret the results. DNA Labs UAE is equipped with the latest in genetic testing technology and staffed by experts in the field, ensuring that patients receive accurate and actionable information about their genetic health.
The DDX3X Gene Mental Retardation X-Linked Type 102 Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the DDX3X gene, which have been associated with X-linked mental retardation type 102. This condition, primarily affecting neurological development, can lead to a range of cognitive impairments and developmental delays, with symptoms and severity varying widely among individuals. The test involves analyzing the patient's DNA to detect any abnormalities or mutations in the DDX3X gene that could be responsible for the condition.
Performed at DNA Labs UAE, a leading facility in genetic diagnostics, this test offers families and individuals crucial information regarding the genetic underpinnings of mental retardation and related developmental issues. The cost of the test is set at 4400 AED, reflecting the advanced technology and expertise required to accurately identify mutations in the DDX3X gene. By opting for this test, patients gain access to critical insights that can guide treatment decisions, inform about potential developmental expectations, and offer a clearer understanding of the genetic factors contributing to the condition.
The UPF3B Gene Mental Retardation X-Linked Type 14 Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the UPF3B gene, which is located on the X chromosome. This gene plays a critical role in the nonsense-mediated mRNA decay pathway, which is essential for normal brain development and function. Mutations in the UPF3B gene have been linked to various neurodevelopmental disorders, including intellectual disability, autism spectrum disorders, and schizophrenia. These conditions are often referred to collectively as X-linked mental retardation type 14.
The test is particularly valuable for families with a history of X-linked intellectual disabilities, providing crucial information for genetic counseling, early intervention, and personalized management plans for affected individuals. Conducted at DNA Labs UAE, a leading facility in genetic testing, the test involves collecting a DNA sample, usually through a blood draw or cheek swab, and analyzing it for specific mutations in the UPF3B gene.
The cost of the UPF3B Gene Mental Retardation X-Linked Type 14 Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the sophisticated technology and expert analysis required to accurately identify mutations in the UPF3B gene. Patients considering this test are advised to consult with a genetic counselor or healthcare provider to understand the implications of the results and the best course of action based on the findings.
